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Journal Abstract Search

153 related items for PubMed ID: 17981209

  • 61.
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  • 62. Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.
    Floris C, Rassu S, Boccone L, Gasperini D, Cao A, Crisponi L.
    Eur J Hum Genet; 2008 Jun; 16(6):696-704. PubMed ID: 18270536
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  • 63. Monochromosome transfer and microarray analysis identify a critical tumor-suppressive region mapping to chromosome 13q14 and THSD1 in esophageal carcinoma.
    Ko JM, Chan PL, Yau WL, Chan HK, Chan KC, Yu ZY, Kwong FM, Miller LD, Liu ET, Yang LC, Lo PH, Stanbridge EJ, Tang JC, Srivastava G, Tsao SW, Law S, Lung ML.
    Mol Cancer Res; 2008 Apr; 6(4):592-603. PubMed ID: 18403638
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  • 69. DNA sequence of the translocation breakpoints in undifferentiated embryonal sarcoma arising in mesenchymal hamartoma of the liver harboring the t(11;19)(q11;q13.4) translocation.
    Rajaram V, Knezevich S, Bove KE, Perry A, Pfeifer JD.
    Genes Chromosomes Cancer; 2007 May; 46(5):508-13. PubMed ID: 17311249
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  • 70. Thymidylate synthetase allelic imbalance in clear cell renal carcinoma.
    Colavito D, Cartei G, Dal Bianco M, Stecca A, Zustovich F, Dalle Carbonare M, Ragazzi E, Farina M, Colombrino E, Leon A.
    Cancer Chemother Pharmacol; 2009 Nov; 64(6):1195-200. PubMed ID: 19306093
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  • 71.
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  • 73. Disruption of sodium bicarbonate transporter SLC4A10 in a patient with complex partial epilepsy and mental retardation.
    Gurnett CA, Veile R, Zempel J, Blackburn L, Lovett M, Bowcock A.
    Arch Neurol; 2008 Apr; 65(4):550-3. PubMed ID: 18413482
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  • 76. Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish family.
    McKay L, Frydenberg M, Lipton L, Norris F, Winship I.
    Fam Cancer; 2011 Jun; 10(2):349-53. PubMed ID: 21188539
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  • 78. Distribution of breakpoints on chromosome 18 in breast, colorectal, and pancreatic carcinoma cell lines.
    Alsop AE, Teschendorff AE, Edwards PA.
    Cancer Genet Cytogenet; 2006 Jan 15; 164(2):97-109. PubMed ID: 16434311
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  • 79. Fluorescent cytogenetics of renal cell neoplasms.
    Brunelli M, Gobbo S, Cossu-Rocca P, Cheng L, Ficarra V, Novara G, Menestrina F, Chilosi M, Martignoni G.
    Pathologica; 2008 Dec 15; 100(6):454-60. PubMed ID: 19475886
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  • 80. Decreased expression of CXXC4 promotes a malignant phenotype in renal cell carcinoma by activating Wnt signaling.
    Kojima T, Shimazui T, Hinotsu S, Joraku A, Oikawa T, Kawai K, Horie R, Suzuki H, Nagashima R, Yoshikawa K, Michiue T, Asashima M, Akaza H, Uchida K.
    Oncogene; 2009 Jan 15; 28(2):297-305. PubMed ID: 18931698
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